Menu
Recruiting NCT06913296

PTeye in Parathyroid Adenoma

Observational Parathyroid Adenoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: parathyroidectomy.
Who it may be relevant to
Registry conditions: Parathyroid Adenoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Greece
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Do PTeye Score Correlate With Biochemical Markers in Parathyroid Adenoma?

Overview

Identifying the parathyroids is compulsory for success of parathyroidectomy for parathyroid adenoma. Near-infrared autofluorescence devices have been proposed as useful intraoperative tools for the identification of parathyroid glands. The aim of the present study is to evaluate the correlation of PTeye autofluorescence device with biochemical data of parathyroid adenoma patients.

Detailed description

Identifying the parathyroids is compulsory for success of parathyroidectomy for parathyroid adenoma. Near-infrared autofluorescence devices have been proposed as useful intraoperative tools for the identification of parathyroid glands. Two approaches are available to surgeons to perform near-infrared autofluorescence: (i) Camera-based systems (CBS) and (ii) Probe-based systems such as PTeye™ (Medtronic, Minneapolis, MN).The aim of the present study is to evaluate the correlation of PTeye autofluorescence device with biochemical data of parathyroid adenoma patients.

Interventions

  • Procedure parathyroidectomy
    typical open parathyroidectomy

Primary outcome measures

  • assess the correlation of PTeye values with biochemical data [Time frame: intraoperatively and 1st postoperative day]

Eligibility criteria

Inclusion criteria

  • Age >18 years old
  • primary hyperparathyroidism caused by adenoma
  • patient's informed consent acquired

Exclusion criteria

  • Secondary and tertiary hyperparathyroidism
  • Re-operation for adenoma
  • Previous neck surgery
  • Patient enrolled in another study that may affect the results of this study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Greece · 1 center
  • Aristotle Univeristy of Thessaloniki — Thessaloniki

Identifiers

NCT: NCT06913296 · PTeye adenoma

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗